Ostravik-Lindemann-Solberg syndrome

Ostravik-Lindemann-Solberg syndrome, also known as heart defect-tongue hamartoma-polysyndactyly syndrome is a rare, multi-systemic genetic disorder which is characterized by congenital heart defects, tongue hamartomas, postaxial polydactyly of the hand, and syndactylism of the foot. This condition is thought to be caused by an autosomal dominant mutation in the WDPCP gene, in chromosome 2.[1][2] Only 5 cases have been recorded in medical literature.[3]

Ostravil-Lindemann-Solberg syndrome
SpecialtyMedical genetics
Symptomscongenital heart defects, polysyndactyly, and tongue hamartomas.
Complicationsdeath
Usual onsetbirth
Durationlife-long
CausesGenetic mutation
Diagnostic methodGenetic testing.
Preventionnone
Frequencyvery rare, only 5 cases have been reported

References

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  1. ^ "Heart defect-tongue hamartoma-polysyndactyly syndrome - About the Disease". Genetic and Rare Diseases Information Center. 2021-01-08. Retrieved 2022-05-13.
  2. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Heart defect tongue hamartoma polysyndactyly syndrome". www.orpha.net.{{cite web}}: CS1 maint: numeric names: authors list (link)
  3. ^ "OMIM Entry - # 217085 - CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY; CHDTHP". omim.org.